Scanlan® SURG-I-LOOP® PLUS with semi-sharp needle 1001-82P

GUDID 00846159000313

Scanlan® SURG-I-LOOP® PLUS with semi-sharp needle - Light Orange, 37cm long, needle 1mm diam (2/pkg)

SCANLAN INTERNATIONAL INC

Surgical vessel loop

• Primary Device ID: 00846159000313
• NIH Device Record Key: ad5cd627-1f00-4ed1-a7c5-b7550998a6f7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Scanlan® SURG-I-LOOP® PLUS with semi-sharp needle
• Version Model Number: 1001-82P
• Catalog Number: 1001-82P
• Company DUNS: 023055619
• Company Name: SCANLAN INTERNATIONAL INC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 651-298-0997
• Email: vanderpoelw@scanlangroup.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00846159000313 [Primary]

FDA Product Code

• GAE: Snare, Surgical

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2020-05-06
• Device Publish Date: 2017-07-21

On-Brand Devices [Scanlan® SURG-I-LOOP® PLUS with semi-sharp needle]

• 00846159027822: Scanlan® SURG-I-LOOP® PLUS with semi-sharp needle - Light Orange, 37cm long, needle 1mm diam,
• 00846159000313: Scanlan® SURG-I-LOOP® PLUS with semi-sharp needle - Light Orange, 37cm long, needle 1mm diam (